Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/6238
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dc.contributor.authorDhanabal, T-
dc.contributor.authorSuresh, T-
dc.contributor.authorMohan, P S-
dc.date.accessioned2009-10-21T07:54:49Z-
dc.date.available2009-10-21T07:54:49Z-
dc.date.issued2006-02-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/6238-
dc.description523-525en_US
dc.description.abstractA simple and one-pot synthesis of 1, 10-diethoxy-1H-pyrano[4, 3-b]quinolines 3a-e from the respective 4-chloro-3-formyl-2-(2-hydroxyethen-1-yl)quinolines 2a-e has been achieved (by Vilsmeier’s reaction on 4-hydroxyquinaldines) by way of intramolecular cyclization when reacted with ethanol in the presence of a few drops of hydrochloric acid. All the newly synthesized compounds have been characterized by their spectral and analytical data. Anti-bacterial studies also have been carried out for some of the synthesized compounds.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 Den_US
dc.sourceIJC-B Vol.45B(02) [February 2006]en_US
dc.subjectHydroxyquinaldinesen_US
dc.subjectVilsmeier Reactionen_US
dc.subjectdiethoxy-1H-pyrano[4, 3-b]quinolinesen_US
dc.subjectanti-bacterial activityen_US
dc.titleSynthesis of new 1, 10-diethoxy-1H-pyrano[4, 3-b]quinolines and their antibacterial studiesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.45B(02) [February 2006]

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